Lot numbers can be found on the outside label of a product:
Please log in for operation!
*For research and further manufacturing use only, not for direct human use.
Structure of 135564-22-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Bromo-3,5-difluorobenzaldehyde features a trifunctional aromatic core with complementary electronic and steric properties. The aldehyde group enables direct coupling in cross-coupling and condensation reactions. Electron-withdrawing bromo and difluoro substituents enhance reactivity in palladium-catalyzed transformations while maintaining stability under standard bench conditions.
4-Bromo-3,5-difluorobenzaldehyde serves as a versatile building block in medicinal chemistry and materials science, enabling efficient construction of complex heterocycles and functionalized aryl scaffolds. Its orthogonal reactivity profile—combining electrophilic bromine and electron-withdrawing fluorine substituents—facilitates palladium-catalyzed cross-coupling and nucleophilic addition reactions with high chemoselectivity. The aldehyde functionality allows for facile derivatization via imine formation, reductive amination, or Grignard additions, while the compound exhibits excellent bench stability and ease of purification, making it well-suited for scalable synthesis and process development workflows.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: